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Research and Characterization of New Genes Involved in Intellectual Disability — GeneDefi  

Intellectual Disability Clinical Trial

Official title:
Recherche et caractérisation de Nouveaux gènes impliqués Dans la déficience Intellectuelle.

Clinical Trial Summary

Intellectual disability (ID) occurs in 2 to 3 % of the general population but the cause is identified only in 30 to 60% of cases.

The purpose of this study is to indentify genes involved in ID with new genetics tools (SNP-arrays, next generation sequencing...) and establish genotype-phenotype correlations.

Clinical Trial Description

n/a

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01867554
Study type Observational
Source Institut National de la Santé Et de la Recherche Médicale, France
Contact Delphine Heron, MD
Phone +33 1 42 16 13 47
Email delphine.heron@psl.aphp.fr
Status Recruiting
Phase N/A
Start date December 2012
Completion date December 2022
View Details
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